ANALYTICAL
STANDARDS
Our laboratory operations are governed by a strict multi-phase verification protocol, ensuring every compound exceeds 99% purity.
01. Synthesis Validation
Synthesis begins with the procurement of high-purity raw amino acids. Each starting material is pre-screened for contaminants before entering the solid-phase peptide synthesis (SPPS) cycle.
02. HPLC / MS Analysis
We utilize High-Performance Liquid Chromatography (HPLC) and Mass Spectrometry (MS)to confirm both the purity and the correct molecular weight of every batch.
How to read our data:
- • Single Sharp Peak: Indicates high purity and absence of co-eluting impurities.
- • Baseline Stability: Confirms the absence of residual solvents or processing chemicals.
- • Mass Spec Match: Confirms the sequence identity matches the target compound exactly.
03. Stability Testing
Lyophilization Quality
Our freeze-drying process removes 99.9% of moisture, creating a stable, "cake-like" structure that prevents peptide degradation during logistics and storage.
Thermal Resistance
Batches are tested under accelerated aging conditions to ensure they maintain structural integrity at varying temperature points.
04. COA Transparency
"Every compound dispatched from our facility includes a verifiable Certificate of Analysis linked directly to the specific batch number."
Authenticated by Third-Party Laboratories